510(k) K092904 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
PATHWAY IVB/VBR
| Applicant | Custom Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Dec 22, 2009 |
| Received | Sep 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092904
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.